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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 262517Generated: October 26, 2026

ethyl (2Z)-3-(pyridin-3-yl)but-2-enoate → HCID 12727116, compound

https://huagongshe.com/reaction/262517

Reaction equation

Participants

RoleNameHCIDCharge
Reactantethyl (2Z)-3-(pyridin-3-yl)but-2-enoateHCID 67402107—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductHCID 12727116HCID 12727116—

Reaction Steps

Ethyl 3-(3-pyridyl)crotonate (prepared from treating 3-acetylpyridine with ethoxycarbonylmethyltriphenylphosphonium bromide and sodium ethoxide) was hydrogenated in ethanol at 40 p.s.i. with 10% palladium on charcoal catalyst to give ethyl 3-(3-pyridyl)butyrate, b.p. 74° /0.15 mmHg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04154834
Source datasetuspto-grants-1979_05
ORD IDord-2cf90d1d47c149628cb15abf2a1798c1
Source noteuspto-grants-1979_05